107367-54-4

Upstream product

• 107367-59-9 2-[(E)-3-(4-Methoxy-phenyl)-acryloylamino]-3-oxo-butyric acid ethyl ester 
• 20207-16-3 ethyl 2-amino-3-oxobutanoate hydrochloride 
• 1198115-57-9 ethyl 2-(2-(4-methoxyphenyl)-1-(phenylsulfonyl)vinyl)-5-methyloxazole-4-carboxylate 
• 34446-64-5 (E)-3-(4-methoxyphenyl)propenoyl chloride 

Downstream Products

• 107367-79-3 {2-[(E)-2-(4-Methoxy-phenyl)-vinyl]-5-methyl-oxazol-4-yl}-acetonitrile 
• 107367-97-5 {2-[(E)-2-(4-Methoxy-phenyl)-vinyl]-5-methyl-oxazol-4-yl}-acetic acid 
• 107390-81-8 {2-[(E)-2-(4-Methoxy-phenyl)-vinyl]-5-methyl-oxazol-4-yl}-methanol 
• 107367-76-0 4-Chloromethyl-2-[(E)-2-(4-methoxy-phenyl)-vinyl]-5-methyl-oxazole 
• 107367-67-9 2-[(E)-2-(4-Methoxy-phenyl)-vinyl]-5-methyl-oxazole-4-carboxylic acid 

Relevant academic research and scientific papers

Development of an oxazole conjunctive reagent and application to the total synthesis of siphonazoles

(Chemical Equation Presented) The preparation of 4-carbethoxy-5-methyl-2- (phenylsulfonyl)methyloxazole and its use in the elaboration of more complex oxazoles are described. A total synthesis of the unique natural products siphonazoles A and B, illustrates an application of this building block. A discussion of the biological activity of the siphonazoles is also presented.